Braze compositions, and related devices

ABSTRACT

A braze alloy composition for sealing a ceramic component to a metal component in an electrochemical cell is presented. The braze alloy composition includes nickel, silicon, boron, and an active metal element. The braze alloy includes nickel in an amount greater than about 50 weight percent, and the active metal element in an amount less than about 10 weight percent. An electrochemical cell using the braze alloy for sealing a ceramic component to a metal component in the cell is also provided.

CROSS REFERENCE TO RELATED APPLICATIONS

This application relates to, and claims priority from, the provisionally filed U.S. patent application having Ser. No. 61/651,817, entitled “COMPOSITIONS FOR BRAZING, AND RELATED METHODS AND DEVICES”, filed on May 25, 2012, which application is hereby incorporated by reference.

TECHNICAL FIELD

This invention generally relates to a braze composition. In some specific embodiments, the invention relates to a braze composition that provides corrosion-resistant sealing and other benefits to high temperature rechargeable batteries.

BACKGROUND OF THE INVENTION

Many types of seal materials have been considered for use in high-temperature rechargeable batteries/cells for joining different components. Sodium/sulfur or sodium/metal halide cells generally include several ceramic and metal components. The ceramic components include an electrically insulating alpha-alumina collar and an ion-conductive electrolyte beta-alumina tube, and are generally joined or bonded via a sealing glass. The metal components include a metallic casing, current collector components, and other metallic components which are often joined by welding or thermal compression bonding (TCB). However, metal-to-ceramic bonding can sometimes present some difficulty, mainly due to thermal stress caused by a mismatch in the coefficient of thermal expansion for the ceramic and metal components.

The metal-to ceramic bonding is most critical for the reliability and safety of the cell. Many types of seal materials and sealing processes have been considered for joining metal to ceramic components, including ceramic adhesives, brazing, and sintering. However, most of the seals may not be able to withstand high temperatures and corrosive environments.

A common bonding technique involves multiple steps of metalizing the ceramic component, followed by bonding the metallized ceramic component to the metal component using a thermal compression bond (TCB). The bond strength of such metal-to-ceramic joints is controlled by a wide range of variables, for example, the microstructure of the ceramic component, the metallization of the ceramic component, and various TCB process parameters. In order to ensure good bond strength, the process requires close control of several parameters involved in various process steps. In short, the method is relatively expensive, and complicated, in view of the multiple processing steps, and the difficulty in controlling the processing steps.

Brazing is another potential technique for making the ceramic-to-metal joints. A braze material is heated above its melting point, and distributed between two or more close-fitting parts by capillary action. However, most of the brazing materials (or braze materials) have limitations that prevent them from fulfilling all of the necessary requirements of high temperature batteries. Moreover, some of the commercial braze materials can be quite expensive themselves; and using them efficiently in various processes can also be costly.

It may be desirable to develop new braze alloy compositions that have properties and characteristics that meet performance requirements for high temperature rechargeable batteries, and are less complicated and less expensive to process, as compared to the existing sealing methods.

BRIEF DESCRIPTION

Various embodiments of the present invention may provide braze alloy compositions for sealing a ceramic to a metal, to form a seal that can withstand corrosive environments.

In accordance with an embodiment of the invention, a braze alloy composition is disclosed, comprising nickel, silicon, boron, and an active metal element. The braze alloy includes nickel in an amount that is usually greater than about 50 weight percent, and the active metal element in an amount up to about 10 weight percent.

In one embodiment, an electrochemical cell incorporating the braze alloy composition is disclosed. The braze alloy includes an active metal element that forms a ceramic-to-metal joint, and has good sodium- and halide-resistance at operating temperatures, along with other complimentary mechanical properties; stability at high temperatures; good thermal expansion properties, and the like. In one embodiment, an energy storage device is also disclosed.

BRIEF DESCRIPTION OF DRAWINGS

These and other features, aspects, and advantages of the present invention will become better understood when the following detailed description is read with reference to the accompanying drawings, wherein:

FIG. 1 is a schematic view showing a cross-section of an electrochemical cell, according to an embodiment;

FIG. 2 depicts X-ray diffraction patterns for two alloy samples; and

FIG. 3 shows scanning electron micrographs of cross-sections of a joint between a ceramic component and a metal component.

DETAILED DESCRIPTION

The invention includes embodiments that relate to a braze alloy composition for sealing an electrochemical cell, for example, a sodium/sulfur or a sodium metal halide battery. The invention also includes embodiments that relate to an electrochemical cell made by using the braze composition. As discussed in detail below, some of the embodiments of the present invention provide a braze alloy for sealing a ceramic component to a metal component, e.g., in an electrochemical cell; along with a metal halide battery formed thereof. These embodiments advantageously provide an improved seal and method for the sealing. Though the present discussion provides examples in the context of a metal halide battery, these processes can be applied to any other application, including ceramic-to-metal or ceramic-to-ceramic joining

When introducing elements of various embodiments of the present invention, the articles “a,” “an,” “the,” and “said” are intended to mean that there are one or more of the elements, unless otherwise indicated. The terms “comprising,” “including,” and “having” are intended to be inclusive, and mean that there may be additional elements other than the listed elements. As used herein, the term “and/or” includes any and all combinations of one or more of the associated listed items. Unless otherwise indicated herein, the terms “disposed on”, “deposited on” or “disposed between” refer to both direct contact between layers, objects, and the like, or indirect contact, e.g., having intervening layers therebetween.

Approximating language, as used herein throughout the specification and claims, may be applied to modify any quantitative representation that could permissibly vary without resulting in a change in the basic function to which it may be related. Accordingly, a value modified by a term such as “about” is not limited to the precise value specified. In some instances, the approximating language may correspond to the precision of an instrument for measuring the value.

As used herein, the term “liquidus temperature” generally refers to a temperature at which an alloy is transformed from a solid into a molten or viscous state. The liquidus temperature specifies the maximum temperature at which crystals can co-exist with the melt in thermodynamic equilibrium. Above the liquidus temperature, the alloy is homogeneous, and below the liquidus temperature, an increasing number of crystals begin to form in the melt with time, depending on the particular alloy. Generally, an alloy, at its liquidus temperature, melts and forms a seal between two components to be joined.

The liquidus temperature can be contrasted with a “solidus temperature”. The solidus temperature quantifies the point at which a material completely solidifies (crystallizes). The liquidus and solidus temperatures do not necessarily align or overlap. If a gap exists between the liquidus and solidus temperatures, then within that gap, the material consists of solid and liquid phases simultaneously (like a “slurry”).

“Sealing” is a function performed by a structure that joins other structures together, to reduce or prevent leakage through the joint between the other structures. The seal structure may also be referred to as a “seal” herein, for the sake of simplicity.

Typically, “brazing” uses a braze material (usually an alloy) having a lower liquidus temperature than the melting points of the components (i.e. their materials) to be joined. The braze material is brought slightly above its melting (or liquidus) temperature while protected by a suitable atmosphere. The braze material then flows over the components (known as wetting), and is then cooled to join the components together. As used herein, “braze alloy composition” or “braze alloy”, “braze material” or “brazing alloy”, refers to a composition that has the ability to wet the components to be joined, and to seal them. A braze alloy, for a particular application, should withstand the service conditions required, and should melt at a lower temperature than the base materials; or should melt at a very specific temperature. Conventional braze alloys usually do not wet ceramic surfaces sufficiently to form a strong bond at the interface of a joint. In addition, the alloys may be prone to sodium and halide corrosion.

As used herein, the term “brazing temperature” refers to a temperature to which a brazing structure is heated to enable a braze alloy to wet the components to be joined, and to form a braze joint or seal. The brazing temperature is often higher than or equal to the liquidus temperature of the braze alloy. In addition, the brazing temperature should be lower than the temperature at which the components to be joined may become chemically, compositionally, and mechanically unstable. There may be several other factors that influence the brazing temperature selection, as those skilled in the art understand.

Embodiments of the present invention provide a braze alloy composition capable of forming a joint by “active brazing” (described below). In some specific embodiments, the composition also has high resistance to sodium and halide corrosion. The braze alloy composition includes nickel, silicon, boron, and an active metal element, as described herein. Each of the elements of the alloy usually contributes and optimizes at least one property of the overall braze composition. These properties may include liquidus temperature, coefficient of thermal expansion, flowability or wettability of the braze alloy with a ceramic; corrosion resistance, and ease-of-processing. Some of the properties are described below.

According to most of the embodiments of the invention, the braze alloy composition is a nickel-based alloy. In other words, the alloy contains a relatively high amount of nickel, as compared to the amount of other elements in the alloy. Nickel is relatively inert in a corrosive environment, as compared to other known base metals, e.g. copper, iron, chromium, cobalt etc. Additionally, it is observed that nickel may enhance other properties of the braze alloy, such as the thermal expansion coefficient, and the phase stability. In general, the amount of nickel balances the alloy based on the amounts of the other constituents. In some embodiments of this invention, a suitable level for the amount of nickel may be at least about 20 weight percent, based on the total weight of the braze alloy. In some embodiments, nickel is present in an amount greater than about 50 weight percent. In some embodiments that are preferred for selective end-use applications, the nickel is present from about 60 weight percent to about 90 weight percent, and in some specific embodiments, from about 70 weight percent to about 80 weight percent, based on the total weight of the braze alloy.

In spite of above discussed properties, nickel-based alloys may have an undesirably high liquidus temperature, i.e., above the required brazing temperature. In order to reduce the liquidus temperature, a melting point depressant may be chosen to form an alloy with nickel, which reduces the melting point of the overall alloy composition. As used herein, the term “melting point depressant” refers to an element or compound which may depress the melting point of the resulting alloy, when added to another element or an alloy. The melting point depressant element may decrease the viscosity and, in turn, increase the flowability (also referred to as wettability) of the braze alloy, at an elevated temperature.

Suitable examples of the melting point depressant include, but are not limited to, silicon, boron, niobium, palladium, or a combination thereof. According to some of the embodiments of the invention, the braze alloy composition includes silicon and boron, and forms a ternary base alloy, i.e., a Ni—Si—B alloy. Any additional melting point depressant may be added to further adjust the liquidus temperature and/or viscosity of the alloy.

The present inventors conceived of a balance of nickel and the melting point depressant (silicon and boron) levels that optimized the liquidus temperature requirements and the requirements for corrosion resistance. A suitable, total amount of the melting point depressant may be up to about 20 weight percent, based on the total weight of the braze alloy. In some specific embodiments, the braze alloy includes from about 1 weight percent to about 10 weight percent silicon, based on the total weight of the braze alloy. In some embodiments, the braze alloy includes up to about 10 weight percent boron, based on the total weight of the braze alloy. A suitable range for each of silicon and boron is often from about 2 weight percent to about 10 weight percent. In some embodiments, a small amount of each of silicon or boron (e.g., less than about 5 weight percent) is used, as each of these may be reactive with the active metal element (e.g. titanium), if present in an amount more than the solubility limit of the element in the alloy.

The braze alloy may include additional melting point depressants, as mentioned above. Examples include niobium and/or palladium. In addition, palladium and niobium may provide good corrosion resistance in a sodium-containing environment. In some embodiments, the braze alloy includes up to about 10 weight percent palladium (e.g., about 0.1 weight percent to about 10 weight percent), based on the total weight of the braze alloy. In some embodiments, the braze alloy includes up to about 5 weight percent niobium (e.g., about 0.1 to about 5 weight percent), based on the total weight of the braze alloy.

As mentioned above, the concept of “active brazing” is important for embodiments of this invention. Active brazing is a technique often used to join a ceramic to a metal, or a ceramic to a ceramic. Active brazing uses an active metal element that promotes wetting of a ceramic surface, enhancing the capability of providing a hermetic seal. An “active metal element”, as used herein, refers to a reactive metal that has high affinity to the oxygen within the ceramic, and thereby reacts with the ceramic. A braze alloy containing an active metal element can also be referred to as an “active braze alloy.” The active metal element undergoes a reaction with the ceramic, when the braze alloy is in a molten state, and leads to the formation of a thin reaction layer on the interface of the ceramic and the braze alloy. The thin reaction layer allows the braze alloy to wet the ceramic surface, resulting in the formation of a ceramic-ceramic or a ceramic-metal joint/bond, which may also be referred to as an “active braze seal.”

Thus, an active metal element is an essential constituent of a braze alloy for employing active brazing. A variety of suitable active metal elements may be used to form the active braze alloy. The selection of a suitable active metal element mainly depends on the chemical reaction with the ceramic (e.g., alumina) to form a uniform and continuous reaction layer, and the capability of the active metal element to form an alloy with a base alloy (e.g. a Ni—Si—B alloy). The active metal element for embodiments herein is often titanium. Other suitable examples of the active metal element include, but are not limited to, zirconium, hafnium, and vanadium. A combination of two or more active metal elements may also be used.

The presence and the amount of the active metal may influence the thickness and the quality of the thin reaction layer, which contributes to the wettability or flowability of the braze alloy, and therefore, the bond strength of the resulting joint. In some embodiments, the active metal is present in an amount less than about 10 weight percent, based on the total weight of the braze alloy. A suitable range is often from about 0.5 weight percent to about 5 weight percent. In some specific embodiments, the active metal is present in an amount ranging from about 1 weight percent to about 3 weight percent, based on the total weight of the braze alloy. The active metal element is generally present in small amounts suitable for improving the wetting of the ceramic surface, and forming the thin reaction layer, for example, less than about 10 microns. A high amount of the active metal layer may cause or accelerate halide corrosion.

The braze alloy composition may further include at least one additional element. The additional element may provide further adjustments in several required properties of the braze alloy, for example, the coefficient of thermal expansion, liquidus temperature, brazing temperature, corrosion resistance, and the strength of the braze alloy. In one embodiment, the additional element (some of which were mentioned above) can include, but is not limited to, iron, chromium, cobalt, niobium, molybdenum, tungsten, or a combination thereof. In some specific embodiments, the braze alloy includes chromium and iron.

With respect to the amount of the additional element(s), the braze alloy includes up to about 10 weight percent (e.g., about 0.1%-10%) of the additional elements, based on the total weight of the braze alloy. In some embodiments, the braze alloy includes up to about 10 weight percent chromium (e.g., about 0.1 to about 10 weight percent), based on the total weight of the braze alloy. In some embodiments, the braze alloy includes from about 0.1 weight percent to about 10 weight percent iron, and in some specific embodiments, up to about 5 weight percent iron, based on the total weight of the braze alloy. In some embodiments, the braze alloy includes from about 0.1 weight percent to about 5 weight percent of molybdenum, based on the total weight of the braze alloy.

In some embodiments, any of the braze alloys described herein may also include cobalt. The addition of cobalt improves the corrosion resistance of the overall composition. The braze alloy may include from about 1 weight percent to about 50 weight percent cobalt, based on the total weight of the braze alloy. In some specific embodiments, the braze alloy includes up to about 10 weight percent of cobalt, based on the total weight of the braze alloy. In some other embodiments, cobalt may replace nickel, and the alloy may be cobalt-based. In these instances, the alloy may include a higher level (from about 40 weight percent to about 80 weight percent) of cobalt, and from about 1 weight percent to about 20 weight percent of nickel.

As mentioned previously, the active metal element usually exhibits relatively high reactivity with each of boron and silicon. The addition of an active metal element like titanium in a braze alloy has been thought to be technically challenging, due to the possibility of titanium boride and titanium silicide formation, which may be undesirable. The formation of these borides and/or silicides may prevent sufficient amounts of titanium from being available for use as the active element. However, for compositions of the present invention, it was observed that the titanium was not “captured” in titanium boride and/or titanium silicide form.

The presence of other elements like nickel, chromium and iron, may avoid the formation of the borides/silicides of the active metal element (i.e., titanium) because of higher reactivity of these elements with boron and/or silicon, than with titanium. Furthermore, the possibility of the formation of titanium boride and/or silicide can also be sometimes avoided by controlled processing of the alloy. For example, during material processing of the alloy into a desired form or shape (e.g., rolling into sheets), when the molten alloy was rapidly quenched, for example by melt spinning, it was observed that the alloy was in the glassy amorphous state, and did not include any boride and/or silicide. FIG. 2 shows X-ray diffraction (XRD) images of two samples formed of alloy compositions, samples 2 and 3, by rapidly quenching during melt spinning. It is clear from the XRDs that the alloys are in an amorphous phase, in both the sheets.

These amorphous alloy samples or “sheets” melt during brazing, and may provide available (free) active metal to react with the ceramic component. Thus, controlled processing of the alloy and brazing process, allows the formation and stabilization of such alloys containing boron, silicon, and titanium.

It may also be possible during the brazing process that the ceramic may react with boron and/or silicon present in the braze alloy, and form an amorphous phase bond. This bond across the ceramic component and the braze alloy may further enhance the strength of the joint.

In one embodiment, the braze alloy includes greater than about 50 weight percent nickel, and between about 1 weight percent and about 10 weight percent of each of silicon, boron, chromium, iron, and an active metal element, based on the total weight of the alloy. In some embodiments for selected end-uses, the braze alloy consists essentially of nickel, chromium, iron, at least one of silicon or boron, and an active metal element. In some preferred embodiments, the active metal element comprises titanium, which may be present in an amount between about 1 weight percent and about 5 weight percent, based on the total weight of the alloy.

As discussed above, the braze alloy has a liquidus temperature lower than the melting temperatures of the components to be joined. In one embodiment, the braze alloy has a liquidus temperature of at least about 850 degrees Celsius. In one embodiment, the braze alloy has a liquidus temperature from about 850 degrees Celsius to about 1300 degrees Celsius, and in some specific embodiments, from about 950 degrees Celsius to about 1250 degrees Celsius.

Some embodiments of the invention provide an electrochemical cell that comprises a first component and a second component joined to each other by a braze alloy composition. The cell may be a sodium-sulfur cell or a sodium-metal halide cell, for example. As described previously, the braze alloy composition includes nickel, silicon, boron, and an active metal element. At least one additional element, such as chromium, iron, niobium, molybdenum, and/or tungsten may further be added. The constituents of the alloy and their respective amounts are described above.

As discussed above, the braze alloy composition may provide an active braze seal to join components in the cell. In one embodiment, the first component of the cell comprises a metal or a metal alloy, and the second component comprises a ceramic. The metal component can be a ring that includes nickel. The ceramic component can be a collar that includes an electrically insulating material, for example alumina.

For example, sodium-sulfur or sodium-metal halide cells may contain the braze alloy composition that forms an active braze seal to form metal-to-ceramic joints. The active braze seal secures an alpha-alumina collar and a nickel ring. FIG. 1 is a schematic diagram depicting an exemplary embodiment of a sodium-metal halide battery cell 10. The cell 10 has an ion-conductive separator tube 20 disposed in a cell case 30. The separator tube 20 is usually made of β-alumina or β″-alumina. The tube 20 defines an anodic chamber 40 between the cell case 30 and the tube 20, and a cathodic chamber 50, inside the tube 30. The anodic chamber 40 is usually filled with an anodic material 45, e.g. sodium. The cathodic chamber 50 contains a cathode material 55 (e.g. nickel and sodium chloride), and a molten electrolyte, usually sodium chloroaluminate (NaAlCl₄).

An electrically insulating ceramic collar 60, which may be made of alpha-alumina, is situated at a top end 70 of the tube 20. A cathode current collector assembly 80 is disposed in the cathode chamber 50, with a cap structure 90, in the top region of the cell. The ceramic collar 60 is fitted onto the top end 70 of the separator tube 20, and is sealed by a glass seal 100. In one embodiment, the cellar 60 includes an upper portion 62, and a lower inner portion 64 that abuts against an inner wall of the tube 20, as illustrated in FIG. 1.

In order to seal the cell 10 at the top end (i.e., its upper region), a metal ring 110 is sometimes disposed. The metal ring 110 has two portions; an outer metal ring 120 and an inner metal ring 130, which are joined, respectively, with the upper portion 62 and the lower portion 64 of the ceramic collar 60, by means of the active braze seals 140 and 150. The active braze seal 140, the seal 150, or both may be formed by using a suitable braze alloy composition described above. The collar 60 and the metal ring 110 may be temporarily held together with an assembly (e.g., a clamp), or by other techniques, until sealing is complete.

The outer metal ring 120 and the inner metal ring 130 are usually welded shut to seal the cell, after joining with the ceramic collar 60 is completed. The outer metal ring 120 can be welded to the cell case 30; and the inner metal ring 130 can be welded to the current collector assembly 80.

The shape and size of the several components discussed above with reference to FIG. 1 are only illustrative for the understanding of the cell structure; and are not meant to limit the scope of the invention. The exact position of the seals and the joined components can vary to some degree. Moreover, each of the terms “collar” and “ring” is meant to comprise metal or ceramic parts of circular or polygonal shape, and in general, all shapes that are compatible with a particular cell design.

The braze alloys and the active braze seal formed thereof, generally have good stability and chemical resistance within determined parameters at a determined temperature. It is desirable (and in some cases, critical) that the braze seal retains its integrity and properties during several processing steps while manufacturing and using the cell, for example, during a glass-seal process for a ceramic-to-ceramic joint, and during operation of the cell. In some instances, optimum performance of the cell is generally obtained at a temperature greater than about 300 degrees Celsius. In one embodiment, the operating temperature may be in a range from about 270 degrees Celsius to about 450 degrees Celsius. In one embodiment, the glass-seal process is carried out at a temperature of at least about 1000 degrees Celsius. In some other embodiments, the glass-seal process is carried out in a range of from about 1000 degrees Celsius to about 1200 degrees Celsius. Moreover, the bond strength and hermeticity of the seal may depend on several parameters, such as the composition of the braze alloy, the thickness of the thin reaction layer, the composition of the ceramic, and the surface properties of the ceramic.

In accordance with some embodiments of this invention, an energy storage device includes a plurality of the electrochemical cells as disclosed in previous embodiments. The cells are, directly or indirectly, in thermal and/or electrical communication with each other. Those of ordinary skill in the art are familiar with the general principles of such devices. For example, U.S. Pat. No. 8,110,301 is illustrative, and incorporated by reference herein. However, there are many other references which generally describe various types of energy storage devices, and their construction.

Some embodiments provide a method for joining a first component to a second component by using a braze alloy composition. The method includes the steps of introducing the braze alloy between the first component and the second component to form a brazing structure. (The alloy could be deposited on one or both of the mating surfaces, for example, as also described below). The brazing structure can then be heated to form an active braze seal between the first component and the second component. In one embodiment, the first component includes a ceramic; and the second component includes a metal. The braze alloy composition includes nickel, silicon, boron, and an active metal element. At least one additional alloying element, such as chromium, palladium, niobium, molybdenum, iron, and/or tungsten, may further be added. The constituents of the braze alloy and their respective amounts (and proportions) are described above.

In the general preparation of the braze alloy, a desired alloy powder mixture may be obtained by combining (e.g., mixing and/or milling) commercial metal powders of the constituents in their respective amounts. In some embodiments, the braze alloy may be employed as a foil, a sheet, a ribbon, a preform, or a wire, or may be formulated into a paste containing water and/or organic fluids. In some embodiments, the precursor metals or metal alloys may be melted to form homogeneous melts, before being formed and shaped into particles. In some cases, the molten material can be directly shaped into foils, preforms or wires. Forming the materials into particles, initially, may comprise spraying the alloy melt into a vacuum, or into an inert gas, to obtain a pre-alloyed powder of the braze alloy. In other cases, pellets of the materials may be milled into a desired particle shape and size.

In one embodiment, a layer of the braze alloy is disposed on at least one surface of the first component or the second component to be joined by brazing. The layer of the braze alloy, in a specific embodiment, is disposed on a surface of the ceramic component. The thickness of the alloy layer may be in a range between about 5 microns and about 300 microns. In some specific embodiments, the thickness of the layer ranges from about 10 microns to about 100 microns. The layer may be deposited or applied on one or both of the surfaces to be joined, by any suitable technique, e.g. by a printing process or other dispensing processes. In some instances, the foil, wire, or the preform may be suitably positioned for bonding the surfaces to be joined.

In some specific embodiments, a sheet or foil of the braze alloy may be desirable. The thickness of the sheets or foils may usually vary between about 20 microns and about 200 microns. The alloys can be rolled into sheets or foils by a suitable technique, for example melt spinning. In one embodiment, the alloy may be melt spun into a sheet or a foil, along with rapid quenching during the spinning

In a typical embodiment, the method further includes the step of heating the brazing structure at the brazing temperature. When the brazing structure is heated at the brazing temperature, the braze alloy melts and flows over the surfaces. The heating can be undertaken in a controlled atmosphere, such as ultra-high pure argon, hydrogen and argon, ultra-high pure helium; or in a vacuum. To achieve good flow and wetting of the braze alloy, the brazing structure is held at the brazing temperature for a few minutes after melting of the braze alloy, and this period may be referred to as the “brazing time”. During the brazing process, a load can also be applied on the samples.

The brazing temperature and the brazing time may influence the quality of the active braze seal. The brazing temperature is generally less than the melting temperatures of the components to be joined, and higher than the liquidus temperature of the braze alloy. In one embodiment, the brazing temperature ranges from about 900 degrees Celsius to about 1500 degrees Celsius, for a time period of about 1 minute to about 30 minutes. In a specific embodiment, the heating is carried out at the brazing temperature from about 1000 degrees Celsius to about 1300 degrees Celsius, for about 5 minutes to about 15 minutes.

During brazing, the alloy melts, and the active metal element (or elements) present in the melt react with the ceramic and form a thin reaction layer at the interface of the ceramic surface and the braze alloy, as described previously. The thickness of the reaction layer may range from about 0.1 micron to about 2 microns, depending on the amount of the active metal element available to react with the ceramic, and depending on the surface properties of the ceramic component. In a typical sequence, the brazing structure is then subsequently cooled to room temperature; with a resulting, active braze seal between the two components. In some instances, rapid cooling of the brazing structure is permitted.

In some embodiments, an additional layer containing the active metal element may be first applied to the ceramic component. The additional layer may have a high amount of the active metal element, for example more than about 70 weight percent. Suitable examples may include nanoparticles of the active metal element, or a hydride of the active metal element, e.g., titanium hydride.

Some of the embodiments of the present invention advantageously provide braze alloys, which are compositionally stable, and chemically stable in the corrosive environment relative to known braze alloys, and are capable of forming an active braze seal for a ceramic-to-metal joint. These braze alloys have high sodium corrosion resistance, and halide corrosion resistance for many end uses. The formation of ceramic-to-metal seals for high temperature cells (as discussed above) by active brazing simplifies the overall cell-assembly process, and improves the reliability and performance of the cell. The present invention provides advantages to leverage a relatively inexpensive, simple, and rapid process to seal the cell or battery, as compared to currently available methods.

EXAMPLES

The examples that follow are merely illustrative, and should not be construed to be any sort of limitation on the scope of the claimed invention. Unless specified otherwise, all ingredients may be commercially available from such common chemical suppliers as Alpha Aesar, Inc. (Ward Hill, Mass.), Sigma Aldrich (St. Louis, Mo.), Spectrum Chemical Mfg. Corp. (Gardena, Calif.), and the like.

Example 1

3 braze alloy compositions (samples 1-3) were prepared. For each braze sample, as shown in Table 1, individual elements were weighed according to the desired composition. These elements were arc-melted to provide an ingot for each composition. To ensure homogeneity of the compositions, the ingots of the samples were triple-melted. The liquidus temperatures of the 3 samples (sample 1, 2, and 3) were measured using Differential Scanning calorimeter (DSC).

TABLE 1 Liquidus Braze Braze alloy composition (weight temperature Samples percent) (° C.) Sample 1 Ni—7Cr—4.5Fe—4.5Si—3.2B—1.25Ti 1069 Sample 2 Ni—7Cr—4.5Fe—4.5Si—3.2B—2Ti 1090 Sample 3 Ni—7Cr—4.5Fe—4.5Si—3.2B—3Ti 1104

Each ingot of samples 2 and 3 was melt-spun into approximately a 75 micron-thick sheet, and rapidly quenched during spinning FIG. 2 shows XRD images of the sample sheets 2, 200 and the sample sheet 3, 202. The XRD images show the presence of the amorphous phase of the alloys in both the sample sheets 2 and 3. These sheets were further measured for elemental analysis by Electron probe micro-analysis (EPMA). The EPMA study confirmed the absence of titanium boride and titanium silicide phases, and indicated the presence of minor amounts of borides and silicides of nickel and chromium.

The sample sheet 2 was then placed between the surfaces of an alpha alumina piece and a nickel piece (parts) to be joined. This assembly was then heated up to about 1200 degrees Celsius for about 10 minutes, and then cooled to room temperature, to form a joint.

FIG. 3 shows cross-sectional SEM images 300 and 400 of the joint in low and high magnification, respectively. SEM image 300 shows a good interface between the alumina piece and the nickel piece. SEM image 400 shows an interface between the alumina piece 402 and braze sample 2, 404, at the joint. A reaction layer 406 was observed between the braze sample 2 and alumina at the braze-ceramic interface, which indicates a reaction between the braze alloy and the ceramic, and the formation of an active braze seal.

While only certain features of the invention have been illustrated and described herein, many modifications and changes will occur to those skilled in the art. It is, therefore, to be understood that the appended claims are intended to cover all such modifications and changes as fall within the true spirit of the invention. 

1. A braze alloy composition, comprising nickel, silicon, boron, and an active metal element, wherein nickel is present in an amount greater than about 50 weight percent, and the active metal element is present in an amount up to about 10 weight percent, based on the total weight of the braze alloy composition.
 2. The braze alloy composition of claim 1, comprising from about 60 weight percent to about 90 weight percent nickel.
 3. The braze alloy composition of claim 1, comprising from about 1 weight percent to about 10 weight percent boron.
 4. The braze alloy composition of claim 1, comprising from about 1 weight percent to about 10 weight percent of silicon.
 5. The braze alloy composition of claim 1, comprising from about 0.5 weight percent to about 5 weight percent of the active metal element.
 6. The braze alloy composition of claim 5, comprising from about 1 weight percent to about 3 weight percent of the active metal element.
 7. The braze alloy composition of claim 1, wherein the active metal element comprises titanium, zirconium, hafnium, vanadium, or a combination thereof.
 8. The braze alloy composition of claim 1, wherein the active metal element comprises titanium.
 9. The braze alloy composition of claim 1, wherein the brazing alloy comprises at least one additional element.
 10. The braze alloy composition of claim 9, wherein the additional element comprises chromium, niobium, cobalt, iron, molybdenum, tungsten, tantalum, or a combination thereof.
 11. The braze alloy composition of claim 10, comprising from about 1 weight percent to about 50 weight percent cobalt.
 12. The braze alloy composition of claim 10, comprising from about 0.1 weight percent to about 10 weight percent chromium.
 13. The braze alloy composition of claim 10, comprising from about 0.1 weight percent to about 10 weight percent iron.
 14. The braze alloy composition of claim 10, comprising from about 0.1 weight percent to about 5 weight percent molybdenum.
 15. The braze alloy composition of claim 1, having a liquidus temperature of at least about 850 degrees Celsius.
 16. The braze alloy composition of claim 15, having a liquidus temperature in a range from about 850 degrees Celsius to about 1250 degrees Celsius.
 17. A braze alloy composition, comprising greater than about 50 weight percent nickel, and from about 1 weight percent to about 10 weight percent each of chromium, iron, silicon, boron, and an active metal element, based on the total weight of the braze alloy composition.
 18. An electrochemical cell, comprising a first component and a second component joined to each other by the braze alloy composition comprising nickel, silicon, boron, and an active metal element, wherein nickel is present in an amount greater than about 50 weight percent, and the active metal element is present in an amount up to about 10 weight percent, based on the total weight of the braze alloy composition.
 19. The electrochemical cell of claim 18, wherein the braze alloy composition provides an active braze seal that joins the first component to the second component.
 20. The electrochemical cell of claim 18, wherein the first component comprises a metal, and the second component comprises a ceramic.
 21. The electrochemical cell of claim 18, wherein the first component comprises nickel.
 22. The electrochemical cell of claim 18, wherein the second component comprises alumina.
 23. An energy storage device comprising a plurality of electrochemical cells as defined in claim
 18. 